Canonical Allele Identifier: CA2959932
Gene: AFP HGNC NCBI

Linked Data

dbSNP Id: rs142106423
ExAC: 4:74307987 T / A
gnomAD v2: 4-74307987-T-A
gnomAD v3: 4-73442270-T-A
gnomAD v4: 4-73442270-T-A
MyVariant Identifiers: chr4:g.74307987T>A (hg19) chr4:g.73442270T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73442270T>A , CM000666.2:g.73442270T>A GRCh38
NC_000004.11:g.74307987T>A , CM000666.1:g.74307987T>A GRCh37
NC_000004.10:g.74526851T>A NCBI36
NG_023028.1:g.11055T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395792.7:c.483-26T>A MANE Select ENSP00000379138.2:n.483-26T>A
ENST00000226359.2:c.483-26T>A ENSP00000226359.2:n.483-26T>A
ENST00000395792.6:c.483-26T>A ENSP00000379138.2:n.483-26T>A
NM_001134.2:c.483-26T>A NP_001125.1:n.483-26T>A
XM_011531704.1:c.480-26T>A XP_011530006.1:n.480-26T>A
NM_001354717.1:c.9-26T>A NP_001341646.1:n.9-26T>A
NM_001134.3:c.483-26T>A MANE Select NP_001125.1:n.483-26T>A
NM_001354717.2:c.9-26T>A NP_001341646.2:n.9-26T>A
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